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JCR 2016
جستجوی مقالات
جمعه 1 اسفند 1404
Iranian Journal of Medical Sciences
، جلد ۴۸، شماره ۵، صفحات ۵۱۶-۵۲۱
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Sporadic Lymphangioleiomyomatosis Disease: A Case Report
چکیده انگلیسی مقاله
Pulmonary Lymphangioleiomyomatosis (LAM) is a rare disease of the lung and lymphatic system that primarily affects women of childbearing age. LAM is a progressive disease with a terrible prognosis, which worsens over time and is extremely difficult to treat. In this study, we discuss the case of a 31-year-old woman with LAM who was initially misdiagnosed with leiomyoma and the way that led to a true diagnosis and effective treatment. Following a precise diagnosis based on comprehensive clinical data and particular immunohistochemical tests, sirolimus treatment was initiated, and the patient entirely responded to the treatment. This case report demonstrated that LAM is an uncommon condition that is challenging to diagnose, which causes its treatment to be delayed.
کلیدواژههای انگلیسی مقاله
Lymphangioleiomyomatosis, Lung, Rare diseases, Pneumothorax
نویسندگان مقاله
Yousef Nikmanesh |
Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
Mansoureh Shokripour |
Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
Maral Mokhtari |
Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
Mahdi Khazayi |
Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran
Ahmad Monabati |
Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
Ramin Rezayi |
Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran
Mehrzad Bahtouee |
Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran
نشانی اینترنتی
https://ijms.sums.ac.ir/article_49115_ff4e7d714ce757d7b5f622c8cbb811e3.pdf
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